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MS Awareness

This is an invisible illness for so many of us – the majority of people with multiple sclerosis (MS) aren’t in a wheelchair and don’t need a walker or even a cane.  We mainly look just like everyone else. Even though I use a cane now, if you put me behind a desk or talk to me on the phone, there is nothing to distinguish me as having something special going on.

And that’s precisely why we need a time like MS Awareness month to ramp up the attention on multiple sclerosis. This isn’t to take away from all the other conditions out there that are equally deserving of awareness and media coverage, but this is our month. March is our time to put Multiple Sclerosis on display.

Awareness is not enough

Not so long ago, awareness seemed to be enough – we wanted to make people aware we have MS. But there is a major shift in priorities and we also now need to promote education, support and acceptance.

If you have MS, you know what I mean. There are so many well-intentioned people out there who think they know what we go through with MS, but as they say… until you walk in our shoes you can’t really know what it’s like to live with this chronic disease. Educating others about what my disease is, continues to be a priority.

Acceptance of people who are different has always been a problem, and acceptance of people with MS is no different. If people are educated about MS, they are more likely to understand and accept the limitations we face and support ways to include us in all facets of life.

How will you help?

How will you observe March and MS Awareness month? I hope your plans include finding ways to let others know more about MS. Or you might take the time to write your elected officials about supporting MS advocacy efforts for healthcare and legislative concerns. Whatever you do, it’s appreciated and helps to complete the MS awareness cycle.

Awareness, education, support and acceptance brings this invisible disease out into the public view, and we all benefit.

Wishing you well,

Laura

This article represents the opinions, thoughts, and experiences of the author; none of this content has been paid for by any advertiser. The MultipleSclerosis.net team does not recommend or endorse any products or treatments discussed herein. Learn more about how we maintain editorial integrity here.

Comments

  • LuvMyDog
    2 years ago

    I was diagnosed with MS nearly 36 years ago. I have found that no matter what I say to people about this disease, it goes in one ear and out the other, with them, adding at the end, “but you look good, you don’t look sick.” Someone just said that to me the other day.
    As far as I’m concerned, no one will ever get it. People who do not have this disease will NEVER understand what it’s like because they are not experiencing it. It’s no different than not knowing what it actually feels like to break your leg in three places and live in a cast for however long, unless it’s actually happened to YOU. I’ve given on the ignorant general public.

  • LuvMyDog
    2 years ago

    “I’ve given up on the general public.” Forgot to add in “up”.

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